arXiv subjects

Maria Dimitrova

Publications and source records attributed to Maria Dimitrova.

5 recordsLinked to original sources

arXiv2025

Magnetically Induced Current Density from Numerical Positional Derivatives of Nucleus Independent Chemical Shifts

Instead of computing magneticallly induced (MI) current densities (CD) via the wave function and their quatum mechanical definition one can also use the differential form of the Amp\`ere-Maxwell law to obtain them from spatial derivatives of the induced magnetic field. In magnetic molecular response calculations, the latter can be done by numerical derivativation of the so called ``nucleus-independent chemical shifts'' (NICS) which are avaialable to many standard quantum chemical programs. The resulting numerical MICD data is in contrast to other numerically obtained MICDs computed via the wave function route, virtually divergence-free.

physics.chem-ph↗

arXiv2021

Current density, current-density pathways and molecular aromaticity

Current densities are induced in the electronic structure of molecules when they are exposed to external magnetic fields. Aromatic molecular rings sustain net diatropic ring currents, whereas the net ring current in antiaromatic molecular rings is paratropic and flows in the opposite, non-classical direction. We present computational methods and protocols to calculate, analyse and visualise magnetically induced current densities in molecules. Calculated ring-current strengths are used for quantifying the degree of aromaticity. The methods have been demonstrated by investigating ring-current strengths and the degree of aromaticity of aromatic, antiaromatic and non-aromatic six-membered hydrocarbon rings. Current-density pathways and ring-current strengths of aromatic and antiaromatic porphyrinoids and other polycyclic molecules have been studied. The aromaticity and current density of M\"obius-twisted molecules has been investigated to find the dependence on the twist and the spatial deformation of the molecular ring. Current densities of fullerene, gaudiene and toroidal carbon nanotubes have also been studied.

physics.chem-ph↗

arXiv2020

Spatial contributions to nuclear magnetic shieldings

We develop a methodology for calculating, analyzing and visualizing nuclear magnetic shielding densities, which are calculated from the current density via the Biot-Savart relation. Atomic contributions to nuclear magnetic shielding constants can be estimated within our framework with a Becke partitioning scheme. The new features have been implemented in the GIMIC program and are applied in this work to the study of the $^1$H and $^{13}$C nuclear magnetic shieldings in benzene (C$_6$H$_6$) and cyclobutadiene (C$_4$H$_4$). The new methodology allows a visual inspection of the spatial origins of the positive (shielding) and negative (deshielding) contributions to the nuclear magnetic shielding constant of a single nucleus, something which has not been hitherto easily accomplished. Analysis of the shielding densities shows that diatropic and paratropic current-density fluxes yield both shielding as well as deshielding contributions, as the shielding or deshielding is determined by the direction of the current-density flux with respect to the studied nucleus instead of the tropicity. Becke partitioning of the magnetic shieldings shows that the magnetic shielding contributions mainly originate from the studied atom and its nearest neighbors, confirming the localized character of nuclear magnetic shieldings.

physics.chem-ph↗

arXiv2020

Benchmarking magnetizabilities with recent density functionals

We have assessed the accuracy for magnetic properties of a set of 51 density functional approximations, including both recently published as well as already established functionals. The accuracy assessment considers a series of 27 small molecules and is based on comparing the predicted magnetizabilities to literature reference values calculated using coupled cluster theory with full singles and doubles and perturbative triples [CCSD(T)] employing large basis sets. The most accurate magnetizabilities, defined as the smallest mean absolute error, were obtained with the BHandHLYP functional. Three of the six studied Berkeley functionals and the three range-separated Florida functionals also yield accurate magnetizabilities. Also some older functionals like CAM-B3LYP, KT1, BHLYP (BHandH), B3LYP and PBE0 perform rather well. In contrast, unsatisfactory performance was generally obtained with Minnesota functionals, which are therefore not recommended for calculations of magnetically induced current density susceptibilities, and related magnetic properties such as magnetizabilities and nuclear magnetic shieldings. We also demonstrate that magnetizabilities can be calculated by numerical integration of the magnetizability density; we have implemented this approach as a new feature in the gauge-including magnetically induced current method (GIMIC). Magnetizabilities can be calculated from magnetically induced current density susceptibilities within this approach even when analytical approaches for magnetizabilities as the second derivative of the energy have not been implemented. The magnetizability density can also be visualized, providing additional information that is not otherwise easily accessible on the spatial origin of the magnetizabilities.

physics.chem-ph↗

arXiv2018

Fully numerical electronic structure calculations on diatomic molecules in weak to strong magnetic fields

We present fully numerical electronic structure calculations on diatomic molecules exposed to an external magnetic field at the unrestricted Hartree-Fock limit, using a modified version of a recently developed finite element program, HelFEM. We have performed benchmark calculations on a few low-lying states of H2, HeH+, LiH, BeH+, BH, and CH+ as a function of the strength of an external magnetic field parallel to the molecular axis. The employed magnetic fields are in the range of $B=[0,10]~B_0$ atomic units, where $B_0 \approx 2.35 \times 10^5$ T. We have compared the results of the fully numerical calculations to ones obtained with the LONDON code using a large uncontracted gauge-including Cartesian Gaussian (GICG) basis set with exponents adopted from the Dunning aug-cc-pVTZ basis set. By comparison to the fully numerical results, we find that the basis set truncation error in the gauge-including Gaussian basis set is of the order of 1 kcal/mol at zero field, that the truncation error grows rapidly when the strength of the magnetic field increases, and that the largest basis set truncation error at $B=10~B_0$ exceeds 1000 kcal/mol. Studies in larger Gaussian basis sets suggest that reliable results can be obtained in GICG basis sets at fields stronger than $B=B_0$, provided that a sufficient coverage of higher-angular-momentum functions is included in the basis set.

physics.chem-ph↗